临床项目经理
Clinical Project Manager
PSI 是一家在行业内拥有 30 年经验的领先合同研究组织，为客户提供稳定与创新完美平衡的服务，同时也为员工提供良好的发展环境。我们专注于在多种治疗领域按时交付高质量的服务。
提升你的职业生涯，领导 II 期和 III 期的全服务临床研究项目，负责整个项目的职责范围，并在研究的每个方面都参与实际操作。
你的职责包括：
· 在直接或一般监督下管理小型项目（<5 个国家和/或有限服务），主要负责按照预定义的质量标准按时按预算完成项目交付物
· 在复杂国际项目/项目中担任区域负责人或项目联合经理的角色，次要负责按照预定义的质量标准按时按预算完成项目交付物
· 遵守并推广与 PSI 客户打交道时的交付和服务原则
· 领导项目团队
· 培训、指导和辅导高级临床监查员 (Lead CRAs)、资深临床监查员 (Senior CRAs)、临床监查员 (CRAs)、项目协调员 (PCAs) 和现场管理专员 (SMAs)
· 参与可行性研究
· 支持业务开发任务，如提案、客户演示、投标答辩会议等
· 实施公司标准流程并遵守部门内部程序
- 本科学历或同等教育、培训和经验组合，具备所需的知识、技能和能力。同等条件定义为至少 5 年在制药/医疗行业和临床研究领域的经验
- 至少 5 年临床研究行业经验
- 最近 2 年在项目经理/同等职位（如临床试验经理、临床研究团队主管等）的临床研究经验
- 具有区域临床项目管理经验，包括从启动到结束的所有项目服务管理
- 在肿瘤学、胃肠病学和/或放射性药物领域有经验者优先
- 优秀的沟通技巧，包括书面和口头表达，能够建立强大的内部和外部利益相关者关系
做出正确的选择，让你的职业生涯迈向全新高度。加入这家重视人才的公司
查看英文原文
PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.
Your responsibilities will include:
· Managing small (<5 countries and/or limited services) projects under direct or general supervision, with primary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget
· Performing regional lead’s or project co-manager’s role in complex international projects/programs with the secondary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget.
· Adhering to and promoting principles of delivery and service in dealing with PSI customers.
· Leading project teams
· Training, mentoring, and coaching Lead CRAs, Senior CRAs, CRAs, Project Coordination Associates (PCAs) and Site Management Associates (SMAs)
· Participating in feasibility research
· Supporting business development tasks such as proposals, client presentations, bid defense meetings, etc.
· Implementing company standard practices and complying with intradepartmental procedures
- Bachelor's degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities. Equivalency is defined as a minimum 5 years of experience gained in pharmaceutical/healthcare industry and clinical research.
- At least 5-year industry experience in clinical research
- At least 2-year recent clinical research experience in the capacity of project manager/equivalent (e.g. Clinical Trial Manager, Clinical Study Team Lead, etc.).
- Regional clinical project management experience, including management of all project services from startup to closure
- Therapeutic experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals is a plus
- Excellent communication skills, both written and verbal, with the ability to build strong internal and external stakeholder relationships
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.